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Front. Immunol. | doi: 10.3389/fimmu.2019.02530

Mucosal Immunity and the FOXO1 Transcription Factor

  • 1University of Pennsylvania, United States

FoxO1 transcription factors affect a number of cell types that are important in the host response. Cell types whose functions are modulated by FoxO1 include keratinocytes in the skin and mucosal dermis, neutrophils and macrophages, dendritic cells, and Tregs and B-cells. FoxO1 is activated by bacterial or cytokine stimulation. Its translocation to the nucleus and binding to promoter regions of genes that have FOXO response elements is stimulated by the MAP kinase pathway and inhibited by the PI3 kinase/Akt pathway. Downstream gene targets of FoxO1 include pro-inflammatory signaling molecules (TLR2, TLR4, IL-1β, TNF-α), wound healing factors (TGF-, VEGF, CTGF) adhesion molecules (integrins-β1, -3, -6, αvβ3, CD11b, CD18 and ICAM-1), chemokine receptors (CCR7 and CXCR2), B cell regulators (APRIL and BLYS), T-regulatory modulators (Foxp3 and CTLA-4), antioxidants (GPX-2 and cytoglobulin) and DNA repair enzymes (Gadd45α). Each of the above cell types are found in periodontal tissues and modulated by bacteria or an inflammatory microenvironment. FoxO1 contributes to the regulation of these cells, which collectively maintain and repair the epithelial barrier, formation and activation of Tregs that are needed to resolve inflammation, mobilization, infiltration and activation of anti-bacterial defenses in neutrophils, and the homing of dendritic cells to lymph nodes to induce T cell and B cell responses. The goal of the manuscript is to review how the transcription factor, FoxO1, contributes to the activation and regulation of key leukocytes needed to maintain homeostasis and respond to bacterial challenge in oral mucosal tissues. Examples are given with an emphasis on lineage specific deletion of FoxO1 to explore the impact of Foxo1 on cell behavior and the impact on inflammation and susceptibility to periodontitis.

Keywords: Bacteria, Gingiva, Mucosa, Forkhead, lymphocyte, PMN (polymorphonuclear leucocyte), Adaptive immune, FOXO (forkhead box protein O)

Received: 25 Jun 2018; Accepted: 11 Oct 2019.

Copyright: © 2019 Graves and Milovanova. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Prof. Dana T. Graves, University of Pennsylvania, Philadelphia, United States,